| scholarly article | Q13442814 |
| P50 | author | David Tilman | Q1176859 |
| Peter B. Reich | Q51690278 | ||
| Dan F.B. Flynn | Q56804570 | ||
| Kevin Mueller | Q57181431 | ||
| Sarah E. Hobbie | Q29834046 | ||
| Forest Isbell | Q40666718 | ||
| Nico Eisenhauer | Q46245773 | ||
| P2860 | cites work | Fire frequency and tree canopy structure influence plant species diversity in a forest-grassland ecotone | Q56965760 |
| Functional diversity (FD), species richness and community composition | Q57067000 | ||
| Rao's quadratic entropy as a measure of functional diversity based on multiple traits | Q57069649 | ||
| The functional role of producer diversity in ecosystems | Q22064504 | ||
| Impacts of plant diversity on biomass production increase through time because of species complementarity | Q24673688 | ||
| COMMUNITY INVASIBILITY, RECRUITMENT LIMITATION, AND GRASSLAND BIODIVERSITY | Q29394552 | ||
| The worldwide leaf economics spectrum | Q29616838 | ||
| Diversity and productivity in a long-term grassland experiment. | Q30756782 | ||
| Elevated CO2 reduces losses of plant diversity caused by nitrogen deposition | Q30959270 | ||
| Plant species richness and functional composition drive overyielding in a six-year grassland experiment | Q30977366 | ||
| Partitioning selection and complementarity in biodiversity experiments | Q30994922 | ||
| BUGS in the analysis of biodiversity experiments: species richness and composition are of similar importance for grassland productivity | Q31002887 | ||
| High plant diversity is needed to maintain ecosystem services | Q31029454 | ||
| Diversity-productivity relationships: initial effects, long-term patterns, and underlying mechanisms | Q33210705 | ||
| Biodiversity and ecosystem stability in a decade-long grassland experiment | Q33245330 | ||
| Niche complementarity for nitrogen: an explanation for the biodiversity and ecosystem functioning relationship? | Q33246144 | ||
| Quantifying the evidence for biodiversity effects on ecosystem functioning and services | Q33257576 | ||
| Biodiversity and ecosystem multifunctionality | Q33290587 | ||
| Janzen-Connell effects are widespread and strong enough to maintain diversity in grasslands | Q33373411 | ||
| Ecological mechanisms associated with the positive diversity-productivity relationship in an N-limited grassland. | Q33422470 | ||
| Species interaction mechanisms maintain grassland plant species diversity | Q33495269 | ||
| Sustaining multiple ecosystem functions in grassland communities requires higher biodiversity | Q33524703 | ||
| From tropics to tundra: global convergence in plant functioning. | Q33722948 | ||
| Plant diversity and the stability of foodwebs | Q33744354 | ||
| Plant diversity and productivity experiments in european grasslands | Q33879171 | ||
| Soil microbes drive the classic plant diversity-productivity pattern | Q33913897 | ||
| Functional and phylogenetic diversity as predictors of biodiversity--ecosystem-function relationships | Q34014811 | ||
| More diverse plant communities have higher functioning over time due to turnover in complementary dominant species | Q34031093 | ||
| Nitrogen limitation constrains sustainability of ecosystem response to CO2. | Q40334408 | ||
| Plant diversity enhances ecosystem responses to elevated CO2 and nitrogen deposition | Q47460581 | ||
| From selection to complementarity: shifts in the causes of biodiversity-productivity relationships in a long-term biodiversity experiment | Q47460583 | ||
| P433 | issue | 6081 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biodiversity | Q47041 |
| biodiversity loss | Q18466271 | ||
| P1104 | number of pages | 4 | |
| P304 | page(s) | 589-592 | |
| P577 | publication date | 2012-05-01 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Impacts of biodiversity loss escalate through time as redundancy fades | |
| P478 | volume | 336 |
| Q34578036 | A comparison of the strength of biodiversity effects across multiple functions |
| Q36178438 | A critical evaluation of ecological indices for the comparative analysis of microbial communities based on molecular datasets. |
| Q57012367 | A general biodiversity-function relationship is mediated by trophic level |
| Q39521515 | A global pattern of thermal adaptation in marine phytoplankton |
| Q51200383 | A horizon scan of global conservation issues for 2013. |
| Q92460271 | A multitrophic perspective on biodiversity-ecosystem functioning research |
| Q55094630 | Aboveground-belowground interactions drive the relationship between plant diversity and ecosystem function |
| Q92568372 | Abrupt declines in marine phytoplankton production driven by warming and biodiversity loss in a microcosm experiment |
| Q28597774 | Adaptation to elevated CO2 in different biodiversity contexts |
| Q35045008 | Advancing biodiversity-ecosystem functioning science using high-density tree-based experiments over functional diversity gradients |
| Q33802140 | Alternative hypotheses to explain why biodiversity-ecosystem functioning relationships are concave-up in some natural ecosystems but concave-down in manipulative experiments |
| Q56984333 | An evolutionary game theoretical model shows the limitations of the additive partitioning method for interpreting biodiversity experiments |
| Q56979827 | An improved model to predict the effects of changing biodiversity levels on ecosystem function |
| Q55312096 | Animal taxa contrast in their scale-dependent responses to land use change in rural Africa. |
| Q97073275 | Applying ecosystem services for pre-market environmental risk assessments of regulated stressors |
| Q92435923 | Assessing the utility of conserving evolutionary history |
| Q35187598 | Biodiversity acts as insurance of productivity of bacterial communities under abiotic perturbations |
| Q58828625 | Biodiversity and ecosystem functioning decoupled: invariant ecosystem functioning despite non-random reductions in consumer diversity |
| Q28603794 | Biodiversity and ecosystem functioning in dynamic landscapes |
| Q31085054 | Biodiversity and ecosystem functioning in evolving food webs. |
| Q54419802 | Biodiversity and multifunctionality in a microbial community: a novel theoretical approach to quantify functional redundancy. |
| Q35579397 | Biodiversity enhances ecosystem multifunctionality across trophic levels and habitats |
| Q28828679 | Biodiversity enhances reef fish biomass and resistance to climate change |
| Q30662922 | Biodiversity ensures plant-pollinator phenological synchrony against climate change. |
| Q89866598 | Biodiversity increases multitrophic energy use efficiency, flow and storage in grasslands |
| Q30938491 | Biodiversity influences plant productivity through niche-efficiency |
| Q34981843 | Biodiversity simultaneously enhances the production and stability of community biomass, but the effects are independent |
| Q26749474 | Biodiversity, ecosystem functioning, and classical biological control |
| Q35105326 | Biodiversity, photosynthetic mode, and ecosystem services differ between native and novel ecosystems |
| Q56996577 | Biodiversity-ecosystem functioning relationships in a long-term non-weeded field experiment |
| Q57281299 | Biodiversity-function relationships in methanogenic communities |
| Q56937602 | Biodiversity–multifunctionality relationships depend on identity and number of measured functions |
| Q70003345 | Biotic interactions, community assembly, and eco-evolutionary dynamics as drivers of long-term biodiversity–ecosystem functioning relationships |
| Q36109965 | Bird assemblage vulnerability depends on the diversity and biogeographic histories of islands |
| Q98196617 | Blind spots in global soil biodiversity and ecosystem function research |
| Q34039678 | Changes in community assembly may shift the relationship between biodiversity and ecosystem function |
| Q35010023 | Changes in the abundance of grassland species in monocultures versus mixtures and their relation to biodiversity effects |
| Q92659566 | Climate-land-use interactions shape tropical mountain biodiversity and ecosystem functions |
| Q99730460 | Co-occurrence history increases ecosystem stability and resilience in experimental plant communities |
| Q34528693 | Coexistence, niches and biodiversity effects on ecosystem functioning |
| Q46259736 | Community evolution increases plant productivity at low diversity. |
| Q63389000 | Compensatory responses can alter the form of the biodiversity–function relation curve |
| Q46274203 | Competitive network determines the direction of the diversity-function relationship |
| Q57179267 | Complementarity in both plant and mycorrhizal fungal communities are not necessarily increased by diversity in the other |
| Q57055692 | Consistent effects of biodiversity loss on multifunctionality across contrasting ecosystems |
| Q30924396 | Constraints to nitrogen acquisition of terrestrial plants under elevated CO2. |
| Q36135655 | Contrasting effects of intra- and interspecific identity and richness of ectomycorrhizal fungi on host plants, nutrient retention and multifunctionality. |
| Q30986763 | Contributions of a global network of tree diversity experiments to sustainable forest plantations |
| Q56965256 | Daily environmental conditions determine the competition-facilitation balance for plant water status |
| Q56965409 | Decade-long soil nitrogen constraint on the CO2 fertilization of plant biomass |
| Q34491607 | Decomposer diversity and identity influence plant diversity effects on ecosystem functioning |
| Q57026610 | Designing forest biodiversity experiments: general considerations illustrated by a new large experiment in subtropical China |
| Q58111246 | Determining the long-term changes in biodiversity and provisioning services along a transect from Central Europe to the Mediterranean |
| Q36243833 | Differential responses and mechanisms of productivity following experimental species loss scenarios |
| Q90289074 | Diversity decoupled from ecosystem function and resilience during mass extinction recovery |
| Q55066352 | Diversity-dependent temporal divergence of ecosystem functioning in experimental ecosystems. |
| Q106351083 | Diversity‐dependent plant–soil feedbacks underlie long‐term plant diversity effects on primary productivity |
| Q56402288 | Do experiments exploring plant diversity-ecosystem functioning relationships inform how biodiversity loss impacts natural ecosystems? |
| Q42372694 | Do temperate tree species diversity and identity influence soil microbial community function and composition? |
| Q35169857 | Does agricultural crop diversity enhance soil microbial biomass and organic matter dynamics? A meta-analysis |
| Q34255771 | Ecology. Impacts of biodiversity loss |
| Q51168996 | Ecology. The heartbeat of ecosystems. |
| Q46242538 | Effects of Plant Functional Group Loss on Soil Microbial Community and Litter Decomposition in a Steppe Vegetation |
| Q56937774 | Effects of biodiversity strengthen over time as ecosystem functioning declines at low and increases at high biodiversity |
| Q34625049 | Effects of plant diversity, N fertilization, and elevated carbon dioxide on grassland soil N cycling in a long-term experiment |
| Q35621652 | Effects of plant diversity, functional group composition, and fertilization on soil microbial properties in experimental grassland |
| Q58727691 | Effects of plant functional traits on soil stability: intraspecific variability matters |
| Q56432915 | Effects of plant litter diversity, species, origin and traits on larval toad performance |
| Q35073421 | Effects of predator richness on prey suppression: a meta-analysis. |
| Q52381770 | Elevated tropospheric CO2 and O3 concentrations impair organic pollutant removal from grassland soil. |
| Q42375788 | Essential Annotation Schema for Ecology (EASE)-A framework supporting the efficient data annotation and faceted navigation in ecology |
| Q30620305 | Evidence of microbial regulation of biogeochemical cycles from a study on methane flux and land use change |
| Q90647681 | Evolution of facilitation requires diverse communities |
| Q35410668 | Evolution of species interactions determines microbial community productivity in new environments |
| Q28647780 | Explaining forest productivity using tree functional traits and phylogenetic information: two sides of the same coin over evolutionary scale? |
| Q57450394 | Fertilizer type and species composition affect leachate nutrient concentrations in coffee agroecosystems |
| Q36199679 | Flood-Induced Changes in Soil Microbial Functions as Modified by Plant Diversity |
| Q46403816 | Food webs obscure the strength of plant diversity effects on primary productivity |
| Q27330346 | Foundation species' overlap enhances biodiversity and multifunctionality from the patch to landscape scale in southeastern United States salt marshes |
| Q34458414 | From stool transplants to next-generation microbiota therapeutics |
| Q56937797 | Functional composition of plant communities determines the spatial and temporal stability of soil microbial properties in a long-term plant diversity experiment |
| Q35659098 | Functional group diversity increases with modularity in complex food webs |
| Q35987812 | Functional identity is the main driver of diversity effects in young tree communities |
| Q56937674 | Functional trait dissimilarity drives both species complementarity and competitive disparity |
| Q33777743 | Functional traits composition predict macrophytes community productivity along a water depth gradient in a freshwater lake |
| Q100427933 | Future climate change vulnerability of endemic island mammals |
| Q35052821 | Genotypic diversity of an invasive plant species promotes litter decomposition and associated processes |
| Q35289962 | Global biodiversity, stoichiometry and ecosystem function responses to human-induced C-N-P imbalances. |
| Q35027576 | Global meta-analysis reveals no net change in local-scale plant biodiversity over time |
| Q41696002 | Herbivore and pathogen effects on tree growth are additive, but mediated by tree diversity and plant traits |
| Q31110758 | Higher levels of multiple ecosystem services are found in forests with more tree species |
| Q90887739 | How do trees respond to species mixing in experimental compared to observational studies? |
| Q35205055 | How much biomass do plant communities pack per unit volume? |
| Q38418068 | Improving intercropping: a synthesis of research in agronomy, plant physiology and ecology. |
| Q35116995 | In a long-term experimental demography study, excluding ungulates reversed invader's explosive population growth rate and restored natives |
| Q58803745 | Increase in soil aggregate stability along a Mediterranean successional gradient in severely eroded gully bed ecosystems: combined effects of soil, root traits and plant community characteristics |
| Q55430474 | Insect community composition and functional roles along a tropical agricultural production gradient. |
| Q57026416 | Interspecific and intraspecific variation in specific root length drives aboveground biodiversity effects in young experimental forest stands |
| Q57020348 | Investigating the relationship between biodiversity and ecosystem multifunctionality: challenges and solutions |
| Q36255576 | Is Variety the Spice of Life? An Experimental Investigation into the Effects of Species Richness on Self-Reported Mental Well-Being |
| Q31120798 | Large-scale variation in combined impacts of canopy loss and disturbance on community structure and ecosystem functioning |
| Q57026424 | Leaf area increases with species richness in young experimental stands of subtropical trees |
| Q90325905 | Limited evidence for spatial resource partitioning across temperate grassland biodiversity experiments |
| Q30376599 | Linking the influence and dependence of people on biodiversity across scales. |
| Q46837543 | Living close to your neighbors: the importance of both competition and facilitation in plant communities |
| Q57268686 | Long-term changes in structure and function of a tropical headwater stream following a disease-driven amphibian decline |
| Q57055703 | Long-term effects of species loss on community properties across contrasting ecosystems |
| Q57026628 | Long-term study of root biomass in a biodiversity experiment reveals shifts in diversity effects over time |
| Q45895724 | Loss of microbial diversity in soils is coincident with reductions in some specialized functions. |
| Q28607248 | Low redundancy in seed dispersal within an island frugivore community |
| Q58107819 | Marine biodiversity and ecosystem functioning: what's known and what's next? |
| Q35734156 | Mechanisms driving diversity-productivity relationships differ between exotic and native communities and are affected by gastropod herbivory |
| Q56938022 | Mechanisms linking plant community properties to soil aggregate stability in an experimental grassland plant diversity gradient |
| Q57424490 | Meeting the Global Ecosystem Collapse Challenge |
| Q64063107 | Meta-analysis shows positive effects of plant diversity on microbial biomass and respiration |
| Q35905961 | Microbial diversity drives multifunctionality in terrestrial ecosystems |
| Q51574146 | Microbial diversity in the cystic fibrosis airways: where is thy sting? |
| Q36097873 | Microbial functional genes enriched in the Xiangjiang River sediments with heavy metal contamination |
| Q38822502 | Microbial therapeutic interventions |
| Q35125698 | Modeled diversity effects on microbial ecosystem functions of primary production, nutrient uptake, and remineralization. |
| Q56879739 | Multiple facets of biodiversity drive the diversity–stability relationship |
| Q36146234 | Multiple metrics of diversity have different effects on temperate forest functioning over succession |
| Q57034128 | Mycorrhiza in tree diversity-ecosystem function relationships: conceptual framework and experimental implementation |
| Q33933170 | New insights into the consequences of post-windthrow salvage logging revealed by functional structure of saproxylic beetles assemblages |
| Q35737030 | No evidence for leaf-trait dissimilarity effects on litter decomposition, fungal decomposers, and nutrient dynamics |
| Q91506208 | Not even wrong: Comment by Wagg et al |
| Q34789120 | Nutrient enrichment, biodiversity loss, and consequent declines in ecosystem productivity |
| Q36050012 | Optimization, validation and efficacy of the phytohaemagglutinin inflammation assay for use in ecoimmunological studies of amphibians |
| Q30977165 | Plant diversity drives soil microbial biomass carbon in grasslands irrespective of global environmental change factors |
| Q35999143 | Plant diversity effects on grassland productivity are robust to both nutrient enrichment and drought |
| Q28707839 | Plant diversity effects on soil food webs are stronger than those of elevated CO2 and N deposition in a long-term grassland experiment |
| Q30984676 | Plant diversity effects on soil microbial functions and enzymes are stronger than warming in a grassland experiment |
| Q34195501 | Plant diversity impacts decomposition and herbivory via changes in aboveground arthropods |
| Q35596157 | Plant diversity increases soil microbial activity and soil carbon storage |
| Q60049453 | Plant diversity maintains multiple soil functions in future environments |
| Q46662654 | Plant diversity shapes microbe-rhizosphere effects on P mobilisation from organic matter in soil |
| Q91599179 | Plant domestication disrupts biodiversity effects across major crop types |
| Q56937915 | Plant identity drives the expression of biocontrol factors in a rhizosphere bacterium across a plant diversity gradient |
| Q57236166 | Plant species richness promotes soil carbon and nitrogen stocks in grasslands without legumes |
| Q88670963 | Plant spectral diversity integrates functional and phylogenetic components of biodiversity and predicts ecosystem function |
| Q56937694 | Plant trait effects on soil organisms and functions |
| Q30313839 | Plants are less negatively affected by flooding when growing in species-rich plant communities |
| Q56937698 | Possible mechanisms underlying abundance and diversity responses of nematode communities to plant diversity |
| Q36836308 | Presence of Trifolium repens Promotes Complementarity of Water Use and N Facilitation in Diverse Grass Mixtures |
| Q38950975 | Press-pulse interactions: effects of warming, N deposition, altered winter precipitation, and fire on desert grassland community structure and dynamics |
| Q57039784 | Progress in the 21st century: a Roadmap for the Ecological Society of Japan |
| Q51150399 | Quantifying effects of biodiversity on ecosystem functioning across times and places. |
| Q35986860 | Recent changes in mountain grasslands: a vegetation resampling study. |
| Q101166728 | Remote spectral detection of biodiversity effects on forest biomass |
| Q56447661 | Resident plant diversity and introduced earthworms have contrasting effects on the success of invasive plants |
| Q34502984 | Response diversity determines the resilience of ecosystems to environmental change |
| Q91225360 | Responses of diversity, productivity, and stability to the nitrogen input in a tropical grassland |
| Q36333564 | Root biomass and exudates link plant diversity with soil bacterial and fungal biomass |
| Q57068945 | Root depth distribution and the diversity–productivity relationship in a long-term grassland experiment |
| Q98776232 | Scaling up biodiversity-ecosystem function relationships across space and over time |
| Q56938071 | Seasonal Variation in the NDVI–Species Richness Relationship in a Prairie Grassland Experiment (Cedar Creek) |
| Q57016461 | Secondary extinctions in food webs: a Bayesian network approach |
| Q35333706 | Selection for niche differentiation in plant communities increases biodiversity effects |
| Q57026644 | Selection in monoculture vs. mixture alters plant metabolic fingerprints |
| Q34981838 | Sensitivity of grassland plant community composition to spatial vs. temporal variation in precipitation |
| Q31000195 | Shifting grassland plant community structure drives positive interactive effects of warming and diversity on aboveground net primary productivity |
| Q57236154 | Soil biota suppress positive plant diversity effects on productivity at high but not low soil fertility |
| Q36198948 | Soil stabilization linked to plant diversity and environmental context in coastal wetlands. |
| Q88081592 | Sown species richness and realized diversity can influence functioning of plant communities differently |
| Q56965162 | Spatial complementarity in tree crowns explains overyielding in species mixtures |
| Q41534209 | Spatially destabilising effect of woody plant diversity on forest productivity in a subtropical mountain forest. |
| Q46333193 | Species richness and traits predict overyielding in stem growth in an early-successional tree diversity experiment |
| Q97538843 | Species richness both impedes and promotes alien plant invasions in the Brazilian Cerrado |
| Q56965289 | Species richness, but not phylogenetic diversity, influences community biomass production and temporal stability in a re-examination of 16 grassland biodiversity studies |
| Q35233051 | Species-level and community-level responses to disturbance: a cross-community analysis. |
| Q114569510 | State of biodiversity documentation in the Philippines: Metadata gaps, taxonomic biases, and spatial biases in the DNA barcode data of animal and plant taxa in the context of species occurrence data |
| Q34459379 | Stress as a modifier of biodiversity effects on ecosystem processes? |
| Q98280916 | Strong positively diversity-productivity relationships in the natural sub-alpine meadow communities across time are up to superior performers |
| Q39136923 | Synthetic microbial ecology and the dynamic interplay between microbial genotypes |
| Q93065539 | Temporal stability of aboveground biomass is governed by species asynchrony in temperate forests |
| Q33804411 | The Intestinal Eukaryotic and Bacterial Biome of Spotted Hyenas: The Impact of Social Status and Age on Diversity and Composition |
| Q35457456 | The biodiversity-dependent ecosystem service debt |
| Q28601786 | The challenges to inferring the regulators of biodiversity in deep time |
| Q36354730 | The economic value of grassland species for carbon storage. |
| Q35844652 | The extent of functional redundancy changes as species' roles shift in different environments |
| Q37490367 | The importance of rare species: a trait-based assessment of rare species contributions to functional diversity and possible ecosystem function in tall-grass prairies |
| Q26782906 | The quest for a mechanistic understanding of biodiversity-ecosystem services relationships |
| Q98665155 | The results of biodiversity-ecosystem functioning experiments are realistic |
| Q63389742 | The strength of the biodiversity-ecosystem function relationship depends on spatial scale |
| Q51455451 | Time-variant species pools shape competitive dynamics and biodiversity-ecosystem function relationships. |
| Q38665780 | To what extent can ecosystem services motivate protecting biodiversity? |
| Q41436927 | Top canopy nitrogen allocation linked to increased grassland carbon uptake in stands of varying species richness |
| Q35690692 | Tree diversity and species identity effects on soil fungi, protists and animals are context dependent |
| Q56937746 | Tree diversity regulates soil respiration through accelerated tree growth in a mesocosm experiment |
| Q51244673 | Understanding the value of plant diversity for ecosystem functioning through niche theory. |
| Q39310248 | Unexpected resilience of a seagrass system exposed to global stressors |
| Q35023749 | Unprecedented carbon accumulation in mined soils: the synergistic effect of resource input and plant species invasion. |
| Q92647200 | Water availability drives aboveground biomass and bird richness in forest restoration plantings to achieve carbon and biodiversity cobenefits |
| Q89896521 | What North America's skeleton crew of megafauna tells us about community disassembly |
| Q92143426 | When Do Ecosystem Services Depend on Rare Species? |
| Q28657356 | Satellites, the all-seeing eyes in the sky: counting elephant seals from space. |
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